Sulphur Liquid
Product Images NDC 15631-2971

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sulphur (NDC 15631-2971). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Carton Box (Dilution Oral Drops Car)

Carton Box (Dilution   Oral Drops   Car)
The packaging label for SULPHUR oral drops, a homeopathic single remedy dilution liquid, displays dosage instructions, warnings, and manufacturer information. The front features the RXHOME© brand logo, a blue flower emblem, and a photo of children playing outdoors. Directions advise adults to take 4 to 6 drops orally three times daily. The label notes the product is distributed by Rxhomeo, Inc in Carrollton, TX, and states that it is manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS). Barcode, QR codes, and batch details placeholders are present on the specimen label panel.*
FDA Label Image

Product Label (Drops Suphur Fda)

Product Label (Drops Suphur Fda)
Label for SULPHUR 1X liquid homeopathic oral solution by Rxhomeo Inc. It lists active ingredients, dosage instructions for adults and children, and notes use for temporary relief of moist skin with acne. The label shows NDC 15631-2971, manufacturing and expiration placeholders, address information, and disclaimers on traditional use and lack of FDA evaluation.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.